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Hemoglobin
international journal for hemoglobin research
Volume 17, 1993 - Issue 5
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Miscellaneous Article

Haplotype-Specific Sequence Variations in the Locus Control Region (5′ Hypersensitive Sites 2, 3, 4) OF βS Chrwosomes

A. D. Adekile Department of Biochemistry and Molecular Biology, Medical College of Georgia, Augusta, GA, 30912-2100, USA
,
A. J. Dimovski Department of Biochemistry and Molecular Biology, Medical College of Georgia, Augusta, GA, 30912-2100, USA
,
C. Oner Department of Biochemistry and Molecular Biology, Medical College of Georgia, Augusta, GA, 30912-2100, USA
,
K. D. Lanclos Department of Biochemistry and Molecular Biology, Medical College of Georgia, Augusta, GA, 30912-2100, USA
&
T. H. J. Huisman Department of Biochemistry and Molecular Biology, Medical College of Georgia, Augusta, GA, 30912-2100, USA
Pages 475-478 | Received 13 Apr 1993, Accepted 06 Jul 1993, Published online: 07 Jul 2009

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Ronald L. Nagel & Martin H. Steinberg. (2001) Role of Epistatic (Modifier) Genes in the Modulation of the Phenotypic Diversity of Sickle Cell Anemia. Pediatric Pathology & Molecular Medicine 20:2, pages 123-136.
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M. H. Steinberg. (1996) Modulation of the Phenotypic Diversity of Sickle Cell Anemia. Hemoglobin 20:1, pages 1-19.
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M. S. Figueirido & M. H. Steinberg. (1996) 5′ Hypersensitive Site-2 and Fetal Hemogln in Brazilians. Hemoglobin 20:4, pages 435-438.
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Articles from other publishers (7)

Adamantia Papachatzopoulou, Polynikis Kaimakis, Farzin Pourfarzad, Panagiotis G. Menounos, Panagiota Evangelakou, Panagoula Kollia, Frank G. Grosveld & George P. Patrinos. (2007) Increased γ‐globin gene expression in β‐thalassemia intermedia patients correlates with a mutation in 3′HS1. American Journal of Hematology 82:11, pages 1005-1009.
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M.S. Gonçalves, G.C. Bomfim, E. Maciel, I. Cerqueira, I. Lyra, A. Zanette, G. Bomfim, E.V. Adorno, A.L. Albuquerque, A. Pontes, M.F. Dupuit, G.B. Fernandes & M.G. dos Reis. (2003) ßS-Haplotypes in sickle cell anemia patients from Salvador, Bahia, Northeastern Brazil. Brazilian Journal of Medical and Biological Research 36:10, pages 1283-1288.
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M. H. Steinberg, Z.‐H. Lu, R. L. Nagel, S. Venkataramani, P. F. Milner, L. Huey, S. Safaya & R. F. Rieder. (1998) Hematological effects of atypical and cameroon β‐globin gene haplotypes in adult sickle cell anemia. American Journal of Hematology 59:2, pages 121-126.
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Maria Plonczynski, Maria Stella Figueiredo & Martin H. Steinberg. (1997) Fetal Hemoglobin in Sickle Cell Anemia: Examination of Phylogenetically Conserved Sequences Within the Locus Control Region but Outside the Cores of Hypersensitive Sites 2 and 3. Blood Cells, Molecules, and Diseases 23:2, pages 188-200.
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J.C. Morgan, D.F. Scott & K.D. Lanclos. (1996) Two mutations in the locus control region hypersensitivity site-2 (5′HS-2) of haplotype 19 βs chromosomes alter binding oftrans-acting factors. American Journal of Hematology 51:1, pages 12-18.
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Martin H. Steinberg. (1994) Sickle Cell Anemia and Fetal Hemoglobin. The American Journal of the Medical Sciences 308:5, pages 259-265.
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D. G. Efremov, A. J. Dimovski, E. Baysal, Z. Ye, A. D. Adekile, M. L. S. Ribeiro, G. Schiliro, Ç. Altay, A. Gürgey, G. D. Efremov & T. H. J. Huisman. (2008) Possible factors influencing the haemoglobin and fetal haemoglobin levels in patients with β‐thalassaemia due to a homozygosity for the IVS‐I‐6 (T→C) mutation. British Journal of Haematology 86:4, pages 824-830.
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